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marker-assisted selection in wheat - ictsd

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Chapter 7 – Marker-<strong>assisted</strong> <strong>selection</strong> <strong>in</strong> common beans and cassava 85Figure 1Examples of gel multiplex<strong>in</strong>g for MAS of A) BGYMV and B) BCMV resistance genesLoad 1S alleleR alleleLoad 2S alleleR alleleLoad 3S alleleR alleleA) bgm-1 geneRS SCAR (Urrea et al., 1996/CIAT)Controls530bp 570bpGel 1Load 2 Load 1 Gel 2Load 3 Load 2 Load 1 Gel 2Load 3Load 2Load 1B) bc-3 geneROC11 SCAR (Johnson et al., 1997)<strong>in</strong>termediate level of resistance, while otherm<strong>in</strong>or genes must be recovered throughconventional phenotypic <strong>selection</strong> to assurehigher resistance.Scal<strong>in</strong>g up of MAS required the developmentof simple operational procedures <strong>in</strong>both the field (tagg<strong>in</strong>g, tissue collection) andthe laboratory (DNA extraction, <strong>marker</strong>evaluation). For gamete <strong>selection</strong> strategies<strong>in</strong> the field, <strong>in</strong>dividual, evenly-spaced plantsfrom segregat<strong>in</strong>g populations were markedwith numbered tags that were coated withparaff<strong>in</strong> to protect them until seed harvest.Leaf disks were sampled from young vegetativetissue with a paper hole puncherand placed directly <strong>in</strong>to pre-numbered cellsof microtitre 96-well plates stored on ice,ready for gr<strong>in</strong>d<strong>in</strong>g and extraction <strong>in</strong> thelaboratory. The implementation of MASfor bgm-1 and subsequently for SW12.700<strong>in</strong> the laboratory required substantial adaptationof standard protocols to establishhigh-throughput procedures. Gr<strong>in</strong>d<strong>in</strong>g ofsamples <strong>in</strong> microtitre plates was accomplishedwith a block of 96 pegs that fit<strong>in</strong>to each well. Alkal<strong>in</strong>e DNA extraction(Klimyuk et al., 1993) was employed withsuccess for both <strong>marker</strong>s, and eventually itwas possible to multiplex the <strong>marker</strong>s <strong>in</strong>both the amplification and gel phases us<strong>in</strong>gmultiple primer PCR and multiple load<strong>in</strong>gper gel wells (Figure 1A). With experienceand improved procedures, efficiency morethan doubled over a two-year period. MASwas often carried out before flower<strong>in</strong>g todecide on a plant’s status as a carrier of theresistant allele for further use <strong>in</strong> cross<strong>in</strong>g.Two small red seeded l<strong>in</strong>es developed <strong>in</strong>the Panamerican School us<strong>in</strong>g MAS havereached the stage of validation <strong>in</strong> Honduras(J.C. Rosas, personal communication) andshown resistance to the BGYMV stra<strong>in</strong>sprevalent there. Resistance to BGYMV ofdrought tolerant l<strong>in</strong>es selected at CIAT wasma<strong>in</strong>ta<strong>in</strong>ed us<strong>in</strong>g MAS for one or moregenes, followed by field <strong>selection</strong> <strong>in</strong> CentralAmerica. Similarly, red mottled l<strong>in</strong>es developed<strong>in</strong> CIAT with the aid of MAS showedfield resistance <strong>in</strong> the Caribbean and one ofthese l<strong>in</strong>es from the red mottled advancedl<strong>in</strong>e for the Caribbean (RMC) series hasbeen released (Blair et al., 2006). MAS hasalso been an important element of ma<strong>in</strong>ta<strong>in</strong><strong>in</strong>gBGYMV viral resistance <strong>in</strong> CIAT’sprogramme as other breed<strong>in</strong>g objectivessuch as nutritional value have beenassumed, necessitat<strong>in</strong>g the <strong>in</strong>clusion of susceptibleparents <strong>in</strong> crosses with resistant

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